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    NDC 68788-7130-04 ALENDRONATE SODIUM 70 mg/1 Details

    ALENDRONATE SODIUM 70 mg/1

    ALENDRONATE SODIUM is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is ALENDRONATE SODIUM.

    Product Information

    NDC 68788-7130
    Product ID 68788-7130_ed6fa6c9-f75d-400a-b68b-b4b24320eda0
    Associated GPIs 30042010100370
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name ALENDRONATE SODIUM
    Proprietary Name Suffix n/a
    Non-Proprietary Name Alendronate sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 70
    Active Ingredient Units mg/1
    Substance Name ALENDRONATE SODIUM
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Bisphosphonate [EPC], Diphosphonates [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076768
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7130-04 (68788713004)

    NDC Package Code 68788-7130-4
    Billing NDC 68788713004
    Package 4 TABLET in 1 BLISTER PACK (68788-7130-4)
    Marketing Start Date 2018-03-30
    NDC Exclude Flag N
    Pricing Information N/A